XIENCE V USA is a prospective, multi-center, multi-cohort post-approval study. The objectives of this study are * To evaluate XIENCE V EECSS continued safety and effectiveness during commercial use in real world settings, and * To support the Food and Drug Administration (FDA) dual antiplatelet therapy (DAPT) initiative. This initiative is designed to evaluate the composite of all death, myocardial infarction (MI) and stroke (MACCE) and the survival of patients that are free from Academic Research Consortium (ARC) definite or probable stent thrombosis (ST) and that have been treated with drug eluting stents (DES) and extended dual antiplatelet therapy.
No linked publications found in PubMed
Inclusion Criteria: * The patient agrees to participate in this study by signing the Institutional Review Board approved informed consent form. Exclusion Criteria: * The inability to obtain an informed consent. * Age limit is determined by investigator. * There are no angiographic inclusion or exclusion criteria for this study.